{"version":"1.0","provider_name":"Geenidiagnostiikka","provider_url":"https:\/\/sites.uef.fi\/genediagnostics","title":"Androgeeniresistenssi - Geenidiagnostiikka","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"bGkJGQAckZ\"><a href=\"https:\/\/sites.uef.fi\/genediagnostics\/monogeeniset-sairaudet\/androgeeniresistenssi\/\">Androgeeniresistenssi<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/sites.uef.fi\/genediagnostics\/monogeeniset-sairaudet\/androgeeniresistenssi\/embed\/#?secret=bGkJGQAckZ\" width=\"600\" height=\"338\" title=\"&#8221;Androgeeniresistenssi&#8221; &#8212; Geenidiagnostiikka\" data-secret=\"bGkJGQAckZ\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script type=\"text\/javascript\">\n\/* <![CDATA[ *\/\n\/*! This file is auto-generated *\/\n!function(d,l){\"use strict\";l.querySelector&&d.addEventListener&&\"undefined\"!=typeof URL&&(d.wp=d.wp||{},d.wp.receiveEmbedMessage||(d.wp.receiveEmbedMessage=function(e){var t=e.data;if((t||t.secret||t.message||t.value)&&!\/[^a-zA-Z0-9]\/.test(t.secret)){for(var s,r,n,a=l.querySelectorAll('iframe[data-secret=\"'+t.secret+'\"]'),o=l.querySelectorAll('blockquote[data-secret=\"'+t.secret+'\"]'),c=new RegExp(\"^https?:$\",\"i\"),i=0;i<o.length;i++)o[i].style.display=\"none\";for(i=0;i<a.length;i++)s=a[i],e.source===s.contentWindow&&(s.removeAttribute(\"style\"),\"height\"===t.message?(1e3<(r=parseInt(t.value,10))?r=1e3:~~r<200&&(r=200),s.height=r):\"link\"===t.message&&(r=new URL(s.getAttribute(\"src\")),n=new URL(t.value),c.test(n.protocol))&&n.host===r.host&&l.activeElement===s&&(d.top.location.href=t.value))}},d.addEventListener(\"message\",d.wp.receiveEmbedMessage,!1),l.addEventListener(\"DOMContentLoaded\",function(){for(var e,t,s=l.querySelectorAll(\"iframe.wp-embedded-content\"),r=0;r<s.length;r++)(t=(e=s[r]).getAttribute(\"data-secret\"))||(t=Math.random().toString(36).substring(2,12),e.src+=\"#?secret=\"+t,e.setAttribute(\"data-secret\",t)),e.contentWindow.postMessage({message:\"ready\",secret:t},\"*\")},!1)))}(window,document);\n\/\/# sourceURL=https:\/\/sites.uef.fi\/genediagnostics\/wp-includes\/js\/wp-embed.min.js\n\/* ]]> *\/\n<\/script>\n","thumbnail_url":"https:\/\/sites.uef.fi\/genediagnostics\/wp-content\/uploads\/sites\/100\/2020\/06\/T321_cmyk_15189-3-e1593515084545.jpg","thumbnail_width":169,"thumbnail_height":107,"description":"T\u00e4ydellisess\u00e4 androgeeniresistenssiss\u00e4 46,XY lapsen ulkoiset sukupuolielimet eiv\u00e4t ole lainkaan maskulinisoituneet vaan lapsen ilmiasu on normaali tyt\u00f6n ilmiasu. Lievemm\u00e4t tautimuodot johtavat eriasteisiin maskulinisaation h\u00e4iri\u00f6ihin (hypospadia, peniksen koon pienuus, kivesten laskeutumattomuus, hedelm\u00e4tt\u00f6myys). Sairauden (OMIM 300068) aiheuttaa geenimuutos X-kromosomissa sijaitsevassa androgeenireseptorigeeniss\u00e4 (AR) (OMIM 313700). Androgeeniresistenssi\u00e4 aiheuttavia geenimuutoksia on kuvattu yli 300, joten geenin sekvensointi on ainut tapa etsi\u00e4 [&hellip;]"}